Ciliary Localization of the Intraflagellar Transport Protein IFT88 Is Disrupted in Cystic Fibrosis
Author:
Affiliation:
1. University of CopenhagenCopenhagen, Denmark
2. Stanford UniversityStanford, Californiaand
3. University of Colorado Anschutz Medical CampusAurora, Colorado
Publisher
American Thoracic Society
Subject
Cell Biology,Clinical Biochemistry,Pulmonary and Respiratory Medicine,Molecular Biology
Reference16 articles.
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3. Cystic Fibrosis
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5. A longitudinal study of lung bacterial pathogens in patients with primary ciliary dyskinesia
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